sypro ruby stain Search Results


sypro ruby protein blot stain  (Bio-Rad)
95
Bio-Rad sypro ruby protein blot stain
Sypro Ruby Protein Blot Stain, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/us10266822-1234-9-14?v=Bio-Rad
Average 95 stars, based on 1 article reviews
sypro ruby protein blot stain - by Bioz Stars, 2026-07
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sypro ruby fluorescent stain  (Bio-Rad)
94
Bio-Rad sypro ruby fluorescent stain
Sypro Ruby Fluorescent Stain, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pmc06265126-226-6-10?v=Bio-Rad
Average 94 stars, based on 1 article reviews
sypro ruby fluorescent stain - by Bioz Stars, 2026-07
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sypro ruby protein blot stain  (Lonza)
90
Lonza sypro ruby protein blot stain
Sypro Ruby Protein Blot Stain, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pmc03305287-64-8-13?v=Lonza
Average 90 stars, based on 1 article reviews
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sypro ruby-stained gel images  (Ludesi AB)
90
Ludesi AB sypro ruby-stained gel images
Sypro Ruby Stained Gel Images, supplied by Ludesi AB, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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sypro ruby staining  (PEQLAB)
90
PEQLAB sypro ruby staining
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Staining, supplied by PEQLAB, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pmc04421866-75-0-18?v=PEQLAB
Average 90 stars, based on 1 article reviews
sypro ruby staining - by Bioz Stars, 2026-07
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sypro ruby fluoresent stain  (Genomic Solutions Inc)
90
Genomic Solutions Inc sypro ruby fluoresent stain
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Fluoresent Stain, supplied by Genomic Solutions Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pm12694396-116-21-25?v=Genomic+Solutions+Inc
Average 90 stars, based on 1 article reviews
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sds-page and sypro ruby staining  (Lonza)
90
Lonza sds-page and sypro ruby staining
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sds Page And Sypro Ruby Staining, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pmc06616311__mmc2-553-13-18?v=Lonza
Average 90 stars, based on 1 article reviews
sds-page and sypro ruby staining - by Bioz Stars, 2026-07
90/100 stars
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sypro ruby-stained slide  (VigeneTech inc)
90
VigeneTech inc sypro ruby-stained slide
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Stained Slide, supplied by VigeneTech inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pmc09451540-432-32-38?v=VigeneTech+inc
Average 90 stars, based on 1 article reviews
sypro ruby-stained slide - by Bioz Stars, 2026-07
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sypro ruby protein gel stain (cat. no. s1200)  (Promega)
90
Promega sypro ruby protein gel stain (cat. no. s1200)
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Protein Gel Stain (Cat. No. S1200), supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pm28442447-60-5-16?v=Promega
Average 90 stars, based on 1 article reviews
sypro ruby protein gel stain (cat. no. s1200) - by Bioz Stars, 2026-07
90/100 stars
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sypro ruby gel stains  (APRO SCIENCE)
90
APRO SCIENCE sypro ruby gel stains
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Gel Stains, supplied by APRO SCIENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pm33997976-73-8-12?v=APRO+SCIENCE
Average 90 stars, based on 1 article reviews
sypro ruby gel stains - by Bioz Stars, 2026-07
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sypro ruby stain  (Fisher Scientific)
86
Fisher Scientific sypro ruby stain
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Stain, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/cheong_han_sian_joshua__2019__abelson_tyrosine_kinase_links_axon_guidance_receptors_to_cytoskeletal_dynamics_through_protein-1615-4-7?v=Fisher+Scientific
Average 86 stars, based on 1 article reviews
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sypro ruby total protein stain  (Mayrhofer Pharmazeutika)
86
Mayrhofer Pharmazeutika sypro ruby total protein stain
Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein <t>(SYPRO</t> <t>Ruby</t> <t>staining).</t> Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.
Sypro Ruby Total Protein Stain, supplied by Mayrhofer Pharmazeutika, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sypro+ruby+stain/pm42289336-247-8-4?v=Mayrhofer+Pharmazeutika
Average 86 stars, based on 1 article reviews
sypro ruby total protein stain - by Bioz Stars, 2026-07
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Image Search Results


Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein (SYPRO Ruby staining). Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.

Journal: Laboratory Investigation; a Journal of Technical Methods and Pathology

Article Title: Critical roles of specimen type and temperature before and during fixation in the detection of phosphoproteins in breast cancer tissues

doi: 10.1038/labinvest.2015.37

Figure Lengend Snippet: Loss of phosphoprotein signal due to delayed preservation (murine samples). Murine breast cancer specimens were either fixed in standard formalin or cold formalin immediately after resection or after different ischemia time points with storage until preservation at room temperature or under vacuum at 4 °C. Protein levels were either determined by reverse phase protein arrays ( a and b ) or by western blot analysis ( c ) with the depicted antibodies. The reverse phase protein arrays data in ( a ) are shown as normalized signal intensities that were calculated by normalization to total protein (SYPRO Ruby staining). Each bar in the reverse phase protein arrays study reflects n =3 data points, besides setting ‘cold formalin, ischemia room temperature', time point 5 h reflects n =4 and time point 24 h reflects n =1. For the setting ‘standard formalin, the ischemia room temperature' time point 24 h is missing because it was not analyzable. In ( b ), two examples (pAKT and pHER2) are highlighted showing the advantage of cold formalin if specimens are kept at 4 °C during the cold ischemia duration. Data are shown as signal intensities in percent relative to the time point zero. Western blot data were normalized to the reference protein beta-Actin before quantification.

Article Snippet: SYPRO Ruby staining was performed according to the manufacturer's instructions and visualized using an E-BOX VX2 UV Transilluminator (Peqlab, Erlangen, Germany).

Techniques: Preserving, Western Blot, Staining

Loss of phosphoprotein signal due to delayed preservation (human samples). Human breast cancer biopsies from six patients were immediately fixed in standard formalin, and matched resection specimens were either fixed in standard formalin or cold formalin. Protein expression was determined by reverse phase protein arrays with depicted antibodies. The reverse phase protein arrays data are depicted as normalized signal intensities, which were calculated by normalization to total protein (SYPRO Ruby staining).

Journal: Laboratory Investigation; a Journal of Technical Methods and Pathology

Article Title: Critical roles of specimen type and temperature before and during fixation in the detection of phosphoproteins in breast cancer tissues

doi: 10.1038/labinvest.2015.37

Figure Lengend Snippet: Loss of phosphoprotein signal due to delayed preservation (human samples). Human breast cancer biopsies from six patients were immediately fixed in standard formalin, and matched resection specimens were either fixed in standard formalin or cold formalin. Protein expression was determined by reverse phase protein arrays with depicted antibodies. The reverse phase protein arrays data are depicted as normalized signal intensities, which were calculated by normalization to total protein (SYPRO Ruby staining).

Article Snippet: SYPRO Ruby staining was performed according to the manufacturer's instructions and visualized using an E-BOX VX2 UV Transilluminator (Peqlab, Erlangen, Germany).

Techniques: Preserving, Expressing, Staining